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1-Palmitoyl-2-Linoleoyl-3-Acetyl-rac-Glycerol Attenuates Streptozotocin-Induced Pancreatic Beta Cell Damage by Promoting Glucose Transporter 2 Endocytosis.
Kim, Jimin; Kim, Joo Heon; Sohn, Ki-Young; Yoon, Sun Young; Kim, Jae Wha.
Afiliación
  • Kim J; Cell Factory Research Center, Division of Systems Biology and Bioengineering, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
  • Kim JH; Department of Functional Genomics, KRIBB School of Bioscience, University of Science and Technology, Daejeon, Republic of Korea.
  • Sohn KY; Department of Pathology, EulJi University School of Medicine, Daejeon, Republic of Korea.
  • Yoon SY; Division of Global New Drug Development, Enzychem Lifesciences, Jecheon, Republic of Korea.
  • Kim JW; Division of Global New Drug Development, Enzychem Lifesciences, Jecheon, Republic of Korea.
Mol Cell Biol ; 39(21)2019 11 01.
Article en En | MEDLINE | ID: mdl-31481450
Streptozotocin (STZ) is widely used to induce diabetic rodent models. It is specifically toxic to pancreatic beta cells and causes severe destruction and dysfunction. We investigated the effect of 1-palmitoyl-2-linoleoyl-3-acetyl-rac-glycerol (PLAG) on an STZ-induced diabetic mouse model. PLAG attenuated the glucose increase and maintained serum insulin at levels similar to those seen with control mice. In pancreatic beta cell line INS-1, STZ-induced cell apoptosis and intracellular reactive oxygen species (ROS) generation were significantly reduced to nearly normal levels after PLAG treatment. Glucose transporter 2 (GLUT2) localization analyses and glucose uptake assays showed that PLAG accelerated GLUT2 internalization, which ameliorated excessive entry of glucose, as well as STZ. STZ-induced cytotoxic effects were significantly reduced in PLAG-treated groups. The biological activity of PLAG was further confirmed in GLUT2-silenced cells, and the specificity of PLAG was verified using its derivative 1-palmitoyl-2-linoleoyl-3-hydroxyl-rac-glycerol (PLH). Our results suggest that PLAG may be a useful agent for protecting beta cells in the setting of excessive glucose influx.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diglicéridos / Células Secretoras de Insulina / Transportador de Glucosa de Tipo 2 Límite: Animals Idioma: En Revista: Mol Cell Biol Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diglicéridos / Células Secretoras de Insulina / Transportador de Glucosa de Tipo 2 Límite: Animals Idioma: En Revista: Mol Cell Biol Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos